levothyroxine sodium

Generic: levothyroxine sodium

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 175 ug/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8811
Product ID 68788-8811_7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211417
Listing Expiration 2026-12-31
Marketing Start 2025-01-20

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888811
Hyphenated Format 68788-8811

Supplemental Identifiers

RxCUI
892246 966222 966249
UNII
9J765S329G

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name levothyroxine sodium (source: ndc)
Generic Name levothyroxine sodium (source: ndc)
Application Number ANDA211417 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 175 ug/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-8811-1)
  • 30 TABLET in 1 BOTTLE (68788-8811-3)
  • 60 TABLET in 1 BOTTLE (68788-8811-6)
  • 90 TABLET in 1 BOTTLE (68788-8811-9)
source: ndc

Packages (4)

68788-8811-1 100 TABLET in 1 BOTTLE (68788-8811-1) 68788-8811-3 30 TABLET in 1 BOTTLE (68788-8811-3) 68788-8811-6 60 TABLET in 1 BOTTLE (68788-8811-6) 68788-8811-9 90 TABLET in 1 BOTTLE (68788-8811-9)

Ingredients (1)

levothyroxine sodium (175 ug/1)

Linked Drug Pages (1)

LEVOTHYROXINE SODIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "966222", "966249"], "spl_set_id": ["7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8811-1)", "package_ndc": "68788-8811-1", "marketing_start_date": "20250120"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8811-3)", "package_ndc": "68788-8811-3", "marketing_start_date": "20250120"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8811-6)", "package_ndc": "68788-8811-6", "marketing_start_date": "20250120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8811-9)", "package_ndc": "68788-8811-9", "marketing_start_date": "20250120"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "68788-8811_7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-8811", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "175 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}